Canonical Allele Identifier: CA1226661613

Gene: AGT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230713513A= , CM000663.2:g.230713513A=	GRCh38
NC_000001.10:g.230849259A= , CM000663.1:g.230849259A=	GRCh37
NC_000001.9:g.228915882A=	NCBI36
NG_008836.1:g.6078T=
NG_008836.2:g.6078T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000366667.6:c.-31+573T= MANE Select	ENSP00000355627.5:n.-31+573T=
ENST00000679684.1:c.-31+573T=	ENSP00000505981.1:n.-31+573T=
ENST00000679738.1:c.-31+573T=	ENSP00000505063.1:n.-31+573T=
ENST00000679802.1:c.-31+573T=	ENSP00000505184.1:n.-31+573T=
ENST00000679854.1:n.481+573T=
ENST00000679957.1:c.-31+573T=	ENSP00000506646.1:n.-31+573T=
ENST00000680041.1:c.-156+573T=	ENSP00000504866.1:n.-156+573T=
ENST00000680783.1:c.-31+573T=	ENSP00000506329.1:n.-31+573T=
ENST00000681269.1:c.-30-2660T=	ENSP00000505985.1:n.-30-2660T=
ENST00000681347.1:n.481+573T=
ENST00000681514.1:c.-117-144T=	ENSP00000505963.1:n.-117-144T=
ENST00000681772.1:c.-31+573T=	ENSP00000505829.1:n.-31+573T=
ENST00000366667.4:c.-4+573T=	ENSP00000355627.4:n.-4+573T=
NM_000029.3:c.-4+573T=	NP_000020.1:n.-4+573T=
NM_000029.4:c.-4+573T=	NP_000020.1:n.-4+573T=
NM_001382817.3:c.-30-2660T=	NP_001369746.2:n.-30-2660T=
NM_001384479.1:c.-31+573T= MANE Select	NP_001371408.1:n.-31+573T=